- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05835947
Anal Cancer Risk In Women
The Role of Early Detection and Treatment of Anal Intraepithelial Neoplasia in the Prevention of Anal Squamous Cell Carcinoma in Women: Establishing the Disease Burden in Women With Genital Cancer
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hypothesis: Women with genital HSILs/SCCs have an increased risk of anal HSIL/SCC regardless of whether they have received treatment for their genital condition and would benefit from surveillance and treatment of anal HSIL in the prevention of ASCC.
This is a retrospective observational (cross sectional) study in which de-personalised patient level National Cancer Registration and Analysis Service data via NHS Digital DARS will be requested.
In particular, patient level data for all women in England, between 2001 and 2019, aged 25- 90+ years, with a diagnosis of anal cancer and/or anal HSIL and:
- vaginal SCC and/or HSIL
- vulvar SCC and/or HSIL
- cervical SCC and/or HSIL
- vaginal and vulvar SCC and/or HSIL
- vaginal and cervical SCC and/or HSIL
- vulvar and cervical SCC and/or HSIL
- vaginal, cervical and vulvar SCC and/or HSIL
For these women with synchronous or metachronous anal and genital HSILs or SCCs data will be collected on:
- Month, Year of each diagnosis.
- Age at each diagnosis.
- Cancer stage (for each cancer): 1, 2, 3, 4, not known, other, unstageable disease.
- Performance status at each diagnosis: 1,2,3,4, not known.
- Treatments received (for each diagnosis): Surgery, Chemotherapy, Radiotherapy.
- Ethnicity: British, Irish, Other white, White/ Black Caribbean, White/Black African, White/ Asian, Other Mixed, Indian, Pakistani, Bangladeshi, Other Asian, Black Caribbean, Black African, Other black, Chinese, Other Ethnic, Not Known.
- Route to Diagnosis (for each diagnosis): Emergency Presentation, GP referral, Inpatient Elective, Other Outpatient, Screening, Two Week Wait, Unknown.
- Deprivation score: 1 (least deprived), 2, 3, 4, 5 (Most deprived).
In order to establish the incidence of anal cancer in women with genital cancers, data will be requested on the total number of women/year (between 2001 and 2019), in England, aged between 25-90+ years with a diagnosis of:
- Anal cancer
- Anal HSIL
- Vulvar cancer
- Vulvar HSIL
- Vaginal cancer
- Vaginal HSIL
- Cervical cancer
- Cervical HSIL
ICD-10 malignant neoplasm and carcinoma in-situ codes will be used to identify these patients:
- Anal Cancer C21.0. C21.1, C21.8
- Cancer of the Vulva C51.0, C51.1, C51.2, C51.8, C51.9
- Cancer of the Vagina C52.
- Cancer of the Cervix Uteri C53.0, C53.1, C53.8, C53.9
- Anal HSIL D01.3
- Vulval HSIL D07.1
- Vaginal HSIL D07.2
- Cervical HSIL D06.0, D06.1, D06.7, D06.9
Primary Objective:
Establish the incidence of anal HSIL and cancer in women with genital HSILs and/cancers and vice versa in England.
Secondary Objectives:
- Asses the risk of anal HSIL and SCC in women with genital HSILs and/or SCC in England.
- Investigate the sociodemographic risk profile of women developing multizonal anogenital HPV driven high-risk pathologies.
- Establish the timelines between the development of genital HSIL/SCC and anal HSIL/SCC.
Primary Outcome:
The incidence of anal HSIL and cancer in women with genital HSIL and/cancer in England between 2001- 2019.
Secondary Outcomes:
- The risk of anal HSIL and/or SCC in women with genital HSILs and/or SCC in England.
- The relationship between the incidence of multizonal anogenital disease and specific sociodemographic risk factors (ethnicity, age, social deprivation).
- The amount of time in years and months between the diagnosis of genital HSIL/SCC and anal HSIL/SCC.
Statistics and Data Analysis:
Data will be analysed using SPSS Statistics software. All outcomes extracted from the database will be expressed in categorical fields; therefore, comparisons of outcomes will be analysed using Chi squared or Fisher's Exact Tests. A statistically significant p value for this analysis is defined as p < 0.05. Incidence will be calculated per 100,000 people per year. Any missing data fields were classified as "unknown" within the database. Missing data will not be excluded from the analysis and "unknown" variables are included with tables and figures to prevent bias.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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-
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London, United Kingdom, SW10 9NH
- Recruiting
- Imperial College London- Chelsea and Westminster NHS Foundation Trust
-
Contact:
- Micol Lupi
- Phone Number: 020 3315 8000
- Email: m.lupi22@imperial.ac.uk
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Women aged 25-90+ years of age.
- Women diagnosed with anal cancer and/or HSIL between 2001 and 2019.
- The anogenital cancer must be a squamous cell carcinoma.
Women with a diagnosis of anal cancer and/or HSIL and:
- vaginal cancer and/ or HSIL
- vulvar cancer and/or HSIL
- cervical cancer and/or HSIL
- vaginal and vulvar cancer and/or HSIL
- vaginal and cervical cancer and/or HSIL
- vulvar and cervical cancer and/or HSIL
- vaginal, cervical and vulvar cancer and/or HSIL
Exclusion Criteria:
- Men with a diagnosis of anal HSIL and/or SCC.
- Women aged outside of the 25-90+ years bracket.
- Women diagnosed with anal cancer or HSIL before 2001 and after 2019.
- Women with genital or anal cancer which is not a squamous cell carcinoma.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The incidence of anal HSIL and cancer in women with genital HSIL and/cancer in England
Time Frame: 2001- 2019
|
as above
|
2001- 2019
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
he risk of anal HSIL and/or SCC in women with genital HSILs and/or SCC in England
Time Frame: 2001-2019
|
as above
|
2001-2019
|
|
The relationship between the incidence of multizonal anogenital disease and specific sociodemographic risk factors.
Time Frame: 2001-2019
|
as above
|
2001-2019
|
|
The amount of time in years and months between the diagnosis of genital HSIL/SCC and anal HSIL/SCC
Time Frame: 2001-2019
|
as above
|
2001-2019
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Digestive System Diseases
- Neoplasms by Histologic Type
- Neoplasms by Site
- Carcinoma
- Neoplasms, Glandular and Epithelial
- Gastrointestinal Neoplasms
- Digestive System Neoplasms
- Gastrointestinal Diseases
- Intestinal Diseases
- Intestinal Neoplasms
- Rectal Diseases
- Colorectal Neoplasms
- Neoplasms, Squamous Cell
- Rectal Neoplasms
- Anus Diseases
- Neoplasms
- Carcinoma in Situ
- Anus Neoplasms
- Papilloma
Other Study ID Numbers
- 315094
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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